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Can a simple drug prevent heart complications during anesthesia?

NCT ID NCT07385040

Symptom relief Sponsor: Shaheed Mohtarma Benazir Bhutto Institue of Trauma Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested two drugs, lignocaine and dexmedetomidine, to see which better prevents sudden rises in heart rate and blood pressure when a breathing tube is inserted during anesthesia. 62 adults having elective surgery took part. The goal is to find a safer way to protect patients, especially those with heart problems, from complications like irregular heartbeat or stroke.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2/3

Runs two stages together: whether the treatment works, then large-scale confirmation.

Participants

62 people

The number who actually took part.

Started

Apr 2023

Finished

Dec 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 60 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Patients undergoing general anesthesia for any elective surgery Having ASA 1 or 2 Having mallapatti 1 or 2 Having BMI in between 18-30 kg/m2 Exclusion Criteria: Lack of consent Anticipated difficult airway Pregnancy Sensitivity to either drug

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Conditions

The condition(s) this trial relates to.

hypertensive disorder Tachycardia

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Hypertension Mean arterial pressure Tachycardia

Contacts and locations

Locations

  • Maryam

    Karachi, Sindh, 7523, Pakistan

More trials for these conditions

Other studies related to the condition(s) this trial covers.